Data Foundry

Medical device recalls 2017

AMT Bridle — Class III medical device recall Z-1223-2017

Terminated recall by Applied Medical Technology Inc, reported 2017-03-01, distributed in AZ, CA, CO, CT, FL, GA, ID, LA…. Expired expiration dates are listed on the pouches.

Recall numberZ-1223-2017
Product typeMedical device
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmApplied Medical Technology Inc, Brecksville, OH, United States
Recall initiated2017-01-19
Classified2017-02-17
Reported by FDA2017-03-01
Terminated2017-12-15
DistributedAZ, CA, CO, CT, FL, GA, ID, LA, ME, MN, MO, NC, OH, OK, OR, TN, TX, UT, WA, WI
Countries outside the USGB
Quantity110
UPC / GTIN / UDI-DI00842071103934, 00842071103941, 00842071103965, 00842071103972, 00842071106638, 00842071106645, 00842071106669, 00842071106676
Lot numbers160926-242, 160930-186, 161007-038, 161010-090, 161014-166, 161018-193, 161019-105, 161021-139
Expiration dates2010-09-01, 2010-10-01, 2019-09-01, 2019-10-01

Product

AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes.

Reason for recall

Expired expiration dates are listed on the pouches.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1223-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.